| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518883 | 0.851 | 0.240 | 15 | 48415571 | missense variant | A/C | snv | 7 | |||
| rs61746008 | 0.882 | 0.160 | 15 | 48412619 | missense variant | G/A;C | snv | 7.3E-04 | 3 |
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057518883 | 0.851 | 0.240 | 15 | 48415571 | missense variant | A/C | snv | 7 | |||
| rs61746008 | 0.882 | 0.160 | 15 | 48412619 | missense variant | G/A;C | snv | 7.3E-04 | 3 |